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2011
Tournament - July 22nd - Registration will Open on April 1st, 2011
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Thank-you
to all of the sponsors and golfers.
$8,575 was raised for charity during the 15th Annual ESAA
Golf Tournament - the Brian Winters Memorial.
In the past 12 years, nearly $39,000 has been raised for charity!
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Artworks
"A charity with the mission of increasing environmental awareness
in Alberta's school system." The Environmental Artworks Foundation
of Alberta (EAFA) is a charitable organization affiliated with The
Environmental Services Association of Alberta (ESAA). In late 2004,
the Association under the direction of the late Brian Winters, and
through his desire that the Association and Industry give back something
to the community that they are a part of, ESAA established EAFA.
EAFA
presents an annual contest to promote environmental artworks in
Alberta.
Two
(2) Mulligans are included with each registration and an additional
$10 from every registration will go towards the Environmental Artworks
Foundation of Alberta. In addition, $25 from each registration is
being donated to Artworks.
Muscular
Dystrophy Canada
Muscular
Dystrophy Canada endeavours to provide relevant and current information
about many types of neuromuscular disorders in an easy to understand
format. For more information visit: www.muscle.ca.
SMA
Spinal
muscular atrophy (SMA) is a term for a group of inherited
neuromuscular diseases. All forms of the disease affect
specialized nerve cells called motor neurons, which control
the movement of voluntary muscles. SMA causes lower motor
neurons in the base of the brain and the spinal cord to
disintegrate, preventing them from delivering electrical
and chemical signals that muscles depend on for normal function.
The three major childhood-onset forms of SMA are now usually
called type 1, type 2 and type 3. SMA type 1 and SBMA affect
the neurons controlling the mouth and throat muscles more
and therefore involve more problems with chewing and swallowing.
Respiratory muscles are involved to varying degrees in all
forms of the disease. In SMA type 1, the most severe form,
the onset of the disease is noted within the first 6 months
of the child's life. Children with SMA type 1 are never
able to sit without support, and death usually occurs before
age 2.
Ilsa
Mae Research Fund
In late 2005, the Chowaniec family and the Environmental
Services Association of Alberta (ESAA), through MDC created
theILSA MAE RESEARCH FUND. This fund has the specific goal
of supporting SMA research in Canada. Money raised for Muscular
Dystrophy Canada at ESAA Events is donated to this fund.
Since the inception of the fund, nearly $80,000 has been
raised for the Fund.
Note:
No cash / ATM Machines on site
- Bring Cash!
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